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在小鼠基因座5'区域鉴定末端脱氧核苷酸转移酶基因的一个新的顺式调控元件。

Identification of a new cis-regulatory element of the terminal deoxynucleotidyl transferase gene in the 5' region of the murine locus.

作者信息

Cherrier Marie, D'Andon Martine Fanton, Rougeon François, Doyen Noëlle

机构信息

Développement des tissus lymphoïdes, Institut Pasteur, 25 rue du Docteur Roux, 75724 Paris Cedex 15, France.

出版信息

Mol Immunol. 2008 Feb;45(4):1009-17. doi: 10.1016/j.molimm.2007.07.027. Epub 2007 Sep 12.

Abstract

Terminal deoxynucleotidyl transferase (TdT) expression is controlled at the transcriptional level, however, the TdT core promoter combining D, D', an initiator (Inr) and downstream basal elements (DBE) does not recapitulate the whole complex regulation of TdT expression. We hypothesized that important cis-regulatory elements of the gene are located outside of the TdT promoter. In an attempt to identify these elements, we performed DNase I hypersensitivity assays over 24kb including a 10kb region located upstream of the transcription start site (+1) and a 14kb region spanning exons and introns I to VI. Hypersensitive sites (HS) HS1 and HS2 were localized 8.5 and 8kb upstream of the transcription start site, respectively, and were exclusively detected in TdT+ cell types. HS3, HS4 and HS5 were mapped at positions -7, -3.4 and -3kb, respectively, and detected in both TdT negative and positive cells. HS6, HS7 and HS8 were detected immediately upstream of the TdT promoter. HS10 and HS11 were localized in the first and third intron of the gene. Luciferase reporter assays revealed that HS1, HS2 and HS3 synergize with the TdT promoter to activate transcription in a TdT+ pre-T cell line but not in a TdT+ pro-B cell line. In summary novel cis-regulatory elements have been identified in the 5' region of the TdT locus that synergize with the promoter to activate gene expression and our results suggest these elements may be more active in T cells.

摘要

末端脱氧核苷酸转移酶(TdT)的表达在转录水平受到调控,然而,结合D、D'、起始子(Inr)和下游基础元件(DBE)的TdT核心启动子并不能概括TdT表达的整个复杂调控过程。我们推测该基因重要的顺式调控元件位于TdT启动子之外。为了鉴定这些元件,我们在包括转录起始位点(+1)上游10kb区域以及跨越外显子和内含子I至VI的14kb区域在内的24kb范围内进行了DNA酶I超敏分析。超敏位点(HS)HS1和HS2分别位于转录起始位点上游8.5kb和8kb处,且仅在TdT阳性细胞类型中检测到。HS3、HS4和HS5分别定位在-7、-3.4和-3kb处,在TdT阴性和阳性细胞中均能检测到。HS6、HS7和HS8在TdT启动子紧邻上游处被检测到。HS10和HS11定位在该基因的第一和第三内含子中。荧光素酶报告基因分析显示,HS1、HS2和HS3与TdT启动子协同作用,在TdT阳性前T细胞系中激活转录,但在TdT阳性前B细胞系中则不然。总之,在TdT基因座的5'区域已鉴定出新型顺式调控元件,它们与启动子协同激活基因表达,我们的结果表明这些元件在T细胞中可能更具活性。

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